The Reaction of Acridine with Methylindole Derivatives

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概要

• 論文の詳細を見る

• It is familiar description of indole in terms of resonance concept that the C3-position of the indole ring has significant high electron density because of the delocalization of electron density from the nitrogen atom to the carbon atoms. In this study, it was clarified that when a mixture of acridine and methylindole derivatives which did not contain the methyl group at C3-position of the indole ring was heated without solvent at 160℃, the products were obtained as the acridine derivatives in high yield. The reaction of 3-methylindole with acridine at 210℃ or above resulted in the formation of the product that C2-position of 3-methylindole was bonded to C9-position of acridine. However, the reaction of 2,3-dimethylindole with acridine did not give condensation product.

• 東海大学の論文

著者

• TAKANO Jiro

  Department of Chemistry, Faculty of Science, Tokai University

• Takano Jiro

  School Of Science Tokai University

• Takano Jiro

  Department Of Chemistry Faculty Of Science Tokai University

• Takano Jiro

  Department Of Biology School Of Education Waseda University

• Kitahara Takio

  School Of Science Tokai University

• Kitahara Takio

  Department Of Chemistry Faculty Of Science Tokai University

• Kitahara T

  School Of Science Tokai University

• Takano J

  School Of Science Tokai University

• ISHIHARA Yoshimi

  School of Science, Tokai University

• Ishihara Yoshimi

  Department of Chemistry, School of Science, Tokai University

• Ishihara Y

  School Of Science Tokai University

• Ishihara Yoshimi

  Department Of Chemistry School Of Science Tokai University

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